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Proteomic strategies: SILAC and 2D-DIGE - powerful tool to investigate cellular alterations.
Methods Mol. Biol. 1101, 369-392 (2014)
Endothelial cells are highly sensitive to high doses of ionizing radiation and the cellular response leads to acute damage of the endothelium. This chapter describes how to measure the effects of ionizing radiation on the proteome of endothelial cells, here showing analysis at 4 and 24 h after exposure. Two complementary proteomic strategies, namely "stable isotope labeling by amino acids in cell culture" (SILAC) and 2D-DIGE analysis are used. In the example given, the exposure triggers considerable alterations in the endothelial protein expression with deregulated proteins categorized into four key pathways: (1) glycolysis/gluconeogenesis, (2) oxidative phosphorylation, (3) Rho-mediated cell motility, and (4) non-homologous end joining (NHEJ). After exposure to high-dose radiation, an immediate down-regulation is seen in the Ku70/Ku80 heterodimer and proliferating cell nuclear antigen (PCNA) proteins belonging to the NHEJ DNA repair pathway. Later time points show significant decrease in the expression levels of proteins of the oxidative phosphorylation (OXPHOS) pathway along with a significant expression increase in the enzymes of the glycolytic pathway. The methods to reproduce our analysis are presented here.
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Publication type
Article: Journal article
Document type
Scientific Article
Editors
Ochs, M.F.*
Keywords
Liquid Chromatography (lc) ; Mass Spectrometry (ms) ; Matrix-assisted Laser-desorption/ Ionization (maldi) ; Oxphos ; Proteomics ; Stable Isotope Labeling Amino Acids In Cell Culture (silac) ; Two-dimensional Difference Gel Electrophoresis (2d-dige)
ISSN (print) / ISBN
1064-3745
e-ISSN
1940-6029
Conference Title
Gene Function Analysis
Journal
Methods in Molecular Biology
Quellenangaben
Volume: 1101,
Pages: 369-392
Publisher
Springer
Publishing Place
Berlin [u.a.]
Reviewing status
Peer reviewed